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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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42 records meeting your search criteria returned- Product Code: OWB Product Problem: No Apparent Adverse Event Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 01/04/2024
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 12/19/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 12/11/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 10/24/2023
SIEMENS HEALTHCARE GMBH-AT ARTIS ZEE III CEILING 07/25/2023
SIEMENS HEALTHCARE GMBH-AT ARTIS ZEE CEILING 05/26/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. AZURION 04/26/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. AZURION 02/24/2023
SIEMENS HEALTHCARE GMBH-AT ARTIS Q BIPLANE 12/20/2021
SIEMENS HEALTHCARE GMBH-AT ARTIS ZEE FLOOR 12/13/2021
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